DISEASES

Disease-gene associations mined from literature

Human genes for glycogen storage disease VI

Glycogen storage disease VI [DOID:2754]

A glycogen storage disease characterized by enlargement of the liver, moderately low blood sugar, elevated levels of acetone and other ketone bodies in the blood and moderate growth retardation.

Synonyms:  glycogen storage disease VI,  DOID:2754,  glycogen storage disease VIs,  glycogen storage disease type VI,  hepatic glycogen phosphorylase deficiency ...

Linkouts:  OMIM